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        If you use plots from MultiQC in a publication or presentation, please cite:

        MultiQC: Summarize analysis results for multiple tools and samples in a single report
        Philip Ewels, Måns Magnusson, Sverker Lundin and Max Käller
        Bioinformatics (2016)
        doi: 10.1093/bioinformatics/btw354
        PMID: 27312411
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        Tool Citations

        Please remember to cite the tools that you use in your analysis.

        To help with this, you can download publication details of the tools mentioned in this report:

        About MultiQC

        This report was generated using MultiQC, version 1.29

        You can see a YouTube video describing how to use MultiQC reports here: https://youtu.be/qPbIlO_KWN0

        For more information about MultiQC, including other videos and extensive documentation, please visit http://multiqc.info

        You can report bugs, suggest improvements and find the source code for MultiQC on GitHub: https://github.com/MultiQC/MultiQC

        MultiQC is published in Bioinformatics:

        MultiQC: Summarize analysis results for multiple tools and samples in a single report
        Philip Ewels, Måns Magnusson, Sverker Lundin and Max Käller
        Bioinformatics (2016)
        doi: 10.1093/bioinformatics/btw354
        PMID: 27312411

        A modular tool to aggregate results from bioinformatics analyses across many samples into a single report.

        Report generated on 2025-09-02, 09:53 CEST based on data in: /Users/adrian/Documents/4 Workspace/Prototipo-resultados/03-EXT-25-Metagenomic/Analisis/miARma_ITS/Pre_fastqc_results

        General Statistics

        Showing 42/42 rows and 3/6 columns.
        Sample NameDupsGCAvg lenMedian lenFailedSeqs
        NGS001-23_ITS2_41_S55_L001_R1_001
        96.2%
        51.0%
        301bp
        301bp
        50%
        0.1M
        NGS001-23_ITS2_41_S55_L001_R2_001
        97.7%
        51.0%
        301bp
        301bp
        58%
        0.1M
        NGS001-23_ITS2_42_S61_L001_R1_001
        95.0%
        49.0%
        301bp
        301bp
        50%
        0.1M
        NGS001-23_ITS2_42_S61_L001_R2_001
        97.1%
        49.0%
        301bp
        301bp
        50%
        0.1M
        NGS001-23_ITS2_43_S67_L001_R1_001
        94.9%
        50.0%
        301bp
        301bp
        50%
        0.1M
        NGS001-23_ITS2_43_S67_L001_R2_001
        96.4%
        51.0%
        301bp
        301bp
        50%
        0.1M
        NGS001-23_ITS2_44_S73_L001_R1_001
        94.3%
        52.0%
        301bp
        301bp
        50%
        0.1M
        NGS001-23_ITS2_44_S73_L001_R2_001
        96.4%
        52.0%
        301bp
        301bp
        42%
        0.1M
        NGS001-23_ITS2_47_S91_L001_R1_001
        95.8%
        51.0%
        301bp
        301bp
        50%
        0.1M
        NGS001-23_ITS2_47_S91_L001_R2_001
        96.9%
        51.0%
        301bp
        301bp
        50%
        0.1M
        NGS001-23_ITS2_48_S97_L001_R1_001
        94.0%
        49.0%
        301bp
        301bp
        42%
        0.0M
        NGS001-23_ITS2_48_S97_L001_R2_001
        96.3%
        50.0%
        301bp
        301bp
        42%
        0.0M
        NGS069-23_ITS2_29_S45_L001_R1_001
        95.4%
        53.0%
        301bp
        301bp
        50%
        0.1M
        NGS069-23_ITS2_29_S45_L001_R2_001
        96.9%
        53.0%
        301bp
        301bp
        50%
        0.1M
        NGS069-23_ITS2_30_S54_L001_R1_001
        95.4%
        50.0%
        301bp
        301bp
        42%
        0.1M
        NGS069-23_ITS2_30_S54_L001_R2_001
        97.3%
        50.0%
        301bp
        301bp
        42%
        0.1M
        NGS069-23_ITS2_31_S63_L001_R1_001
        95.8%
        48.0%
        301bp
        301bp
        42%
        0.1M
        NGS069-23_ITS2_31_S63_L001_R2_001
        97.2%
        48.0%
        301bp
        301bp
        58%
        0.1M
        NGS069-23_ITS2_32_S72_L001_R1_001
        95.1%
        51.0%
        301bp
        301bp
        42%
        0.1M
        NGS069-23_ITS2_32_S72_L001_R2_001
        97.0%
        51.0%
        301bp
        301bp
        42%
        0.1M
        NGS069-23_ITS2_35_S26_L001_R1_001
        96.0%
        51.0%
        301bp
        301bp
        50%
        0.1M
        NGS069-23_ITS2_35_S26_L001_R2_001
        97.4%
        51.0%
        301bp
        301bp
        50%
        0.1M
        NGS069-23_ITS2_36_S37_L001_R1_001
        96.6%
        50.0%
        301bp
        301bp
        50%
        0.1M
        NGS069-23_ITS2_36_S37_L001_R2_001
        97.9%
        50.0%
        301bp
        301bp
        58%
        0.1M
        NGS069-24-ITS2-1_S192_L001_R1_001
        92.9%
        52.0%
        294bp
        294bp
        58%
        0.0M
        NGS069-24-ITS2-1_S192_L001_R2_001
        93.0%
        52.0%
        297bp
        301bp
        58%
        0.0M
        NGS069-24-ITS2-2_S197_L001_R1_001
        93.0%
        52.0%
        294bp
        294bp
        58%
        0.0M
        NGS069-24-ITS2-2_S197_L001_R2_001
        93.2%
        52.0%
        296bp
        301bp
        67%
        0.0M
        NGS069-24-ITS2-3_S202_L001_R1_001
        92.9%
        52.0%
        294bp
        301bp
        58%
        0.0M
        NGS069-24-ITS2-3_S202_L001_R2_001
        93.0%
        51.0%
        297bp
        301bp
        58%
        0.0M
        NGS069-24-ITS2-4_S207_L001_R1_001
        92.8%
        51.0%
        296bp
        301bp
        50%
        0.0M
        NGS069-24-ITS2-4_S207_L001_R2_001
        92.1%
        50.0%
        297bp
        301bp
        58%
        0.0M
        NGS069-24-ITS2-5_S211_L001_R1_001
        93.1%
        51.0%
        296bp
        301bp
        50%
        0.0M
        NGS069-24-ITS2-5_S211_L001_R2_001
        92.5%
        50.0%
        297bp
        301bp
        67%
        0.0M
        NGS069-24-ITS2-6_S215_L001_R1_001
        92.4%
        50.0%
        296bp
        301bp
        50%
        0.0M
        NGS069-24-ITS2-6_S215_L001_R2_001
        91.8%
        50.0%
        297bp
        301bp
        67%
        0.0M
        NGS069-24-ITS2-7_S220_L001_R1_001
        93.4%
        52.0%
        295bp
        301bp
        50%
        0.0M
        NGS069-24-ITS2-7_S220_L001_R2_001
        93.4%
        51.0%
        297bp
        301bp
        58%
        0.0M
        NGS069-24-ITS2-8_S225_L001_R1_001
        93.7%
        50.0%
        296bp
        301bp
        50%
        0.0M
        NGS069-24-ITS2-8_S225_L001_R2_001
        93.2%
        50.0%
        297bp
        301bp
        58%
        0.0M
        NGS069-24-ITS2-9_S193_L001_R1_001
        92.9%
        51.0%
        295bp
        301bp
        50%
        0.0M
        NGS069-24-ITS2-9_S193_L001_R2_001
        92.6%
        50.0%
        297bp
        301bp
        58%
        0.0M

        FastQC

        Version: 0.11.5

        Quality control tool for high throughput sequencing data.URL: http://www.bioinformatics.babraham.ac.uk/projects/fastqc

        Sequence Counts

        Sequence counts for each sample. Duplicate read counts are an estimate only.

        This plot show the total number of reads, broken down into unique and duplicate if possible (only more recent versions of FastQC give duplicate info).

        You can read more about duplicate calculation in the FastQC documentation. A small part has been copied here for convenience:

        Only sequences which first appear in the first 100,000 sequences in each file are analysed. This should be enough to get a good impression for the duplication levels in the whole file. Each sequence is tracked to the end of the file to give a representative count of the overall duplication level.

        The duplication detection requires an exact sequence match over the whole length of the sequence. Any reads over 75bp in length are truncated to 50bp for this analysis.

        Created with MultiQC

        Sequence Quality Histograms

        The mean quality value across each base position in the read.

        To enable multiple samples to be plotted on the same graph, only the mean quality scores are plotted (unlike the box plots seen in FastQC reports).

        Taken from the FastQC help:

        The y-axis on the graph shows the quality scores. The higher the score, the better the base call. The background of the graph divides the y axis into very good quality calls (green), calls of reasonable quality (orange), and calls of poor quality (red). The quality of calls on most platforms will degrade as the run progresses, so it is common to see base calls falling into the orange area towards the end of a read.

        Created with MultiQC

        Per Sequence Quality Scores

        The number of reads with average quality scores. Shows if a subset of reads has poor quality.

        From the FastQC help:

        The per sequence quality score report allows you to see if a subset of your sequences have universally low quality values. It is often the case that a subset of sequences will have universally poor quality, however these should represent only a small percentage of the total sequences.

        Created with MultiQC

        Per Base Sequence Content

        The proportion of each base position for which each of the four normal DNA bases has been called.

        To enable multiple samples to be shown in a single plot, the base composition data is shown as a heatmap. The colours represent the balance between the four bases: an even distribution should give an even muddy brown colour. Hover over the plot to see the percentage of the four bases under the cursor.

        To see the data as a line plot, as in the original FastQC graph, click on a sample track.

        From the FastQC help:

        Per Base Sequence Content plots out the proportion of each base position in a file for which each of the four normal DNA bases has been called.

        In a random library you would expect that there would be little to no difference between the different bases of a sequence run, so the lines in this plot should run parallel with each other. The relative amount of each base should reflect the overall amount of these bases in your genome, but in any case they should not be hugely imbalanced from each other.

        It's worth noting that some types of library will always produce biased sequence composition, normally at the start of the read. Libraries produced by priming using random hexamers (including nearly all RNA-Seq libraries) and those which were fragmented using transposases inherit an intrinsic bias in the positions at which reads start. This bias does not concern an absolute sequence, but instead provides enrichement of a number of different K-mers at the 5' end of the reads. Whilst this is a true technical bias, it isn't something which can be corrected by trimming and in most cases doesn't seem to adversely affect the downstream analysis.

        Click a sample row to see a line plot for that dataset.
        Rollover for sample name
        Position: -
        %T: -
        %C: -
        %A: -
        %G: -

        Per Sequence GC Content

        The average GC content of reads. Normal random library typically have a roughly normal distribution of GC content.

        From the FastQC help:

        This module measures the GC content across the whole length of each sequence in a file and compares it to a modelled normal distribution of GC content.

        In a normal random library you would expect to see a roughly normal distribution of GC content where the central peak corresponds to the overall GC content of the underlying genome. Since we don't know the GC content of the genome the modal GC content is calculated from the observed data and used to build a reference distribution.

        An unusually shaped distribution could indicate a contaminated library or some other kinds of biased subset. A normal distribution which is shifted indicates some systematic bias which is independent of base position. If there is a systematic bias which creates a shifted normal distribution then this won't be flagged as an error by the module since it doesn't know what your genome's GC content should be.

        Created with MultiQC

        Per Base N Content

        The percentage of base calls at each position for which an N was called.

        From the FastQC help:

        If a sequencer is unable to make a base call with sufficient confidence then it will normally substitute an N rather than a conventional base call. This graph shows the percentage of base calls at each position for which an N was called.

        It's not unusual to see a very low proportion of Ns appearing in a sequence, especially nearer the end of a sequence. However, if this proportion rises above a few percent it suggests that the analysis pipeline was unable to interpret the data well enough to make valid base calls.

        Created with MultiQC

        Sequence Length Distribution

        The distribution of fragment sizes (read lengths) found. See the FastQC help

        Created with MultiQC

        Sequence Duplication Levels

        The relative level of duplication found for every sequence.

        From the FastQC Help:

        In a diverse library most sequences will occur only once in the final set. A low level of duplication may indicate a very high level of coverage of the target sequence, but a high level of duplication is more likely to indicate some kind of enrichment bias (e.g. PCR over amplification). This graph shows the degree of duplication for every sequence in a library: the relative number of sequences with different degrees of duplication.

        Only sequences which first appear in the first 100,000 sequences in each file are analysed. This should be enough to get a good impression for the duplication levels in the whole file. Each sequence is tracked to the end of the file to give a representative count of the overall duplication level.

        The duplication detection requires an exact sequence match over the whole length of the sequence. Any reads over 75bp in length are truncated to 50bp for this analysis.

        In a properly diverse library most sequences should fall into the far left of the plot in both the red and blue lines. A general level of enrichment, indicating broad oversequencing in the library will tend to flatten the lines, lowering the low end and generally raising other categories. More specific enrichments of subsets, or the presence of low complexity contaminants will tend to produce spikes towards the right of the plot.

        Created with MultiQC

        Overrepresented sequences by sample

        The total amount of overrepresented sequences found in each library.

        FastQC calculates and lists overrepresented sequences in FastQ files. It would not be possible to show this for all samples in a MultiQC report, so instead this plot shows the number of sequences categorized as overrepresented.

        Sometimes, a single sequence may account for a large number of reads in a dataset. To show this, the bars are split into two: the first shows the overrepresented reads that come from the single most common sequence. The second shows the total count from all remaining overrepresented sequences.

        From the FastQC Help:

        A normal high-throughput library will contain a diverse set of sequences, with no individual sequence making up a tiny fraction of the whole. Finding that a single sequence is very overrepresented in the set either means that it is highly biologically significant, or indicates that the library is contaminated, or not as diverse as you expected.

        FastQC lists all the sequences which make up more than 0.1% of the total. To conserve memory only sequences which appear in the first 100,000 sequences are tracked to the end of the file. It is therefore possible that a sequence which is overrepresented but doesn't appear at the start of the file for some reason could be missed by this module.

        Created with MultiQC

        Top overrepresented sequences

        Top overrepresented sequences across all samples. The table shows 20 most overrepresented sequences across all samples, ranked by the number of samples they occur in.

        Showing 20/20 rows and 3/3 columns.
        Overrepresented sequenceReportsOccurrences% of all reads
        TCCTCCGCTTATTGATATGCTTAAGTTCAGCGGGTATCCCTACCTGATCC
        21
        408559
        17.3703%
        GTGAGTCATCGAATCTTTGAACGCACATTGCGCCCGCCAGTATTCTGGCG
        21
        82334
        3.5005%
        GTGAATCATCGAATCTTTGAACGCACATTGCGCCCGCCAGTATTCTGGCG
        21
        65616
        2.7897%
        GTGAGTCATCGAATCTTTGAACGCACATTGCGCCCTATGGTATTCCGTAG
        21
        54684
        2.3250%
        GTGAGTCATCGAATCTTTGAACGCACATTGCGCCCCTTGGTATTCCATGG
        21
        53845
        2.2893%
        GTGAATCATCGAATCTTTGAACGCACATTGCGCCCTATGGTATTCCGTAG
        21
        44554
        1.8943%
        GTGAATCATCGAATCTTTGAACGCACATTGCGCCCCTTGGTATTCCATGG
        21
        36922
        1.5698%
        GTGAGTCATCGAATCTTTGAACGCACATTGCGCCCTTTGGTATTCCTTAG
        21
        32602
        1.3861%
        GTGAATCATCGAATCTTTGAACGCACATTGCGCCCTTTGGTATTCCTTAG
        21
        27090
        1.1518%
        GTGAATCATCGAATCTTTGAACGCACATTGCGCCCCCTGGTATTCCGGGG
        21
        26367
        1.1210%
        GTGAGTCATCGAATCTTTGAACGCACATTGCGCCTTCTGGTATTCCGGGA
        21
        21442
        0.9116%
        GTGAGTCATCGAATCTTTGAACGCACCTTGCGCTCCTTGGTATTCCGAGG
        21
        20223
        0.8598%
        GTGAATCATCGAATCTTTGAACGCACATTGCGCCTTCTGGTATTCCGGGA
        21
        17952
        0.7632%
        GTGAGTCATCGAATCTTTGAACGCACCTTGCGCTCCTTGGTATTCCTTGG
        21
        17539
        0.7457%
        GTGAATCATCGAATCTTTGAACGCACCTTGCGCTCCTTGGTATTCCTTGG
        21
        14869
        0.6322%
        GTGAATCATCGAATCTTTGAACGCACCTTGCGCTCCTTGGTATTCCGAGG
        21
        14793
        0.6289%
        GTGAGTCATCGAATCTTTGAACGCATATTGCGCTCTCTGGTATTCCGGAG
        21
        11206
        0.4764%
        GTGAGTCATCGAATCTTTGAACGCACATTGCGCTTCCTGGTATTCCGGGG
        21
        9531
        0.4052%
        GTGAATCATCGAATCTTTGAACGCATATTGCGCTCTCTGGTATTCCGGAG
        21
        8548
        0.3634%
        GTGAGTCATCGAATCTTTGAACGCACATTGCGCCCCCTGGCATTCCGGGG
        21
        5345
        0.2272%

        Adapter Content

        The cumulative percentage count of the proportion of your library which has seen each of the adapter sequences at each position.

        Note that only samples with ≥ 0.1% adapter contamination are shown.

        There may be several lines per sample, as one is shown for each adapter detected in the file.

        From the FastQC Help:

        The plot shows a cumulative percentage count of the proportion of your library which has seen each of the adapter sequences at each position. Once a sequence has been seen in a read it is counted as being present right through to the end of the read so the percentages you see will only increase as the read length goes on.

        Created with MultiQC

        Status Checks

        Status for each FastQC section showing whether results seem entirely normal (green), slightly abnormal (orange) or very unusual (red).

        FastQC assigns a status for each section of the report. These give a quick evaluation of whether the results of the analysis seem entirely normal (green), slightly abnormal (orange) or very unusual (red).

        It is important to stress that although the analysis results appear to give a pass/fail result, these evaluations must be taken in the context of what you expect from your library. A 'normal' sample as far as FastQC is concerned is random and diverse. Some experiments may be expected to produce libraries which are biased in particular ways. You should treat the summary evaluations therefore as pointers to where you should concentrate your attention and understand why your library may not look random and diverse.

        Specific guidance on how to interpret the output of each module can be found in the relevant report section, or in the FastQC help.

        In this heatmap, we summarise all of these into a single heatmap for a quick overview. Note that not all FastQC sections have plots in MultiQC reports, but all status checks are shown in this heatmap.

        Created with MultiQC

        Software Versions

        Software Versions lists versions of software tools extracted from file contents.

        SoftwareVersion
        FastQC0.11.5